Search Results - "Gaggero, Nicoletta"
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Synthesis of 3,4-Dihydropyridin-2-ones via Domino Reaction under Phase Transfer Catalysis Conditions
Published in Catalysts (01-01-2023)“…3,4-dihydropyridin-2-ones are of considerable importance due to the large number of these core structures exhibiting a diverse array of biological and…”
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2
Building Up Quaternary Stereocenters Through Biocatalyzed Direct Insertion of Carbon Nucleophiles on Ketones
Published in European journal of organic chemistry (19-12-2019)“…Quaternary stereocenters are privileged structural motifs, widely distributed in natural products and in pharmaceutically active compounds. Asymmetric methods…”
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3
Fluorous Biphasic Catalytic Oxidation of Sulfides by Molecular Oxygen/2,2-Dimethylpropanal
Published in European journal of organic chemistry (01-01-2001)“…The use of perfluoroalkyl‐substituted cobalt complexes as catalysts for the oxidation of alkyl aryl sulfides with molecular oxygen/2,2‐dimethypropanal has been…”
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4
Comparison of cyclohexanone monooxygenase as an isolated enzyme and whole cell biocatalyst for the enantioselective oxidation of 1,3-dithiane
Published in Journal of molecular catalysis. B, Enzymatic (01-12-2004)“…Both whole cells of recombinant Escherichia coli TOP10, overexpressing cyclohexanone monooxygenase (CHMO) and isolated cyclohexanone monooxygenase, were used…”
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5
N-Heterocyclic Carbene Catalysis as a Tool for Gaining Access to the 3,4-Dihydropyran-2-one Skeleton
Published in European journal of organic chemistry (01-09-2014)“…An overview of the progress made in the synthesis of 3,4‐dihydropyran‐2‐ones since the development of NHC catalysis is reported. Two distinct classes of…”
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6
Stereoselective reaction of 2-carboxythioesters-1,3-dithiane with nitroalkenes: an organocatalytic strategy for the asymmetric addition of a glyoxylate anion equivalent
Published in Organic & biomolecular chemistry (28-05-2015)“…An efficient organocatalytic methodology has been developed to perform the stereoselective addition of 2-carboxythioesters-1,3-dithiane to nitroalkenes. Under…”
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7
A new approach to 4,6-disubstituted-3,4-dihydropyran-2-ones by Domino Michael addition-cyclization reaction under PTC conditions
Published in Tetrahedron (11-11-2014)“…Domino Michael addition-cyclization reactions of α,β-unsaturated carbonyl compounds with activated 1,3-dithiane-2-carbothioate esters under solid-liquid phase…”
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8
Stereoselective thio-Michael addition to chalcones in water catalyzed by bovine serum albumin
Published in Tetrahedron: asymmetry (2011)“…A biomimetic, inexpensive, and simple method for the stereoselective thio-Michael addition of thiols to chalcones has been developed using bovine serum albumin…”
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9
Recent biotechnological developments in the use of peroxidases
Published in Trends in Biotechnology (01-04-1999)“…Peroxidases are ubiquitous oxidoreductases that use hydrogen peroxide or alkyl peroxides as oxidants. Advances have recently been made in using them to…”
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10
First asymmetric epoxidation catalysed by cyclohexanone monooxygenase
Published in Tetrahedron letters (04-03-2002)Get full text
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11
Microbiological transformations 36: Preparative scale synthesis of chiral thioacetal and thioketal sulfoxides using whole-cell biotransformations
Published in Tetrahedron (14-07-1997)“…This work describes the preparative scale enantioselective oxidation of some prochiral dithioacetals and dithioketals to their corresponding chiral…”
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12
Facile conversion of sulfilimines into sulfoximines using dioxiranes
Published in Tetrahedron letters (04-08-1997)“…Employing dimethyldioxirane, the direct conversion of several N-( p-tolylsulfonyl)sulfilimines and of one N-(acetyl)sulfilimine into the corresponding…”
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13
Chloroperoxidase-catalyzed enantioselective oxidation of methyl phenyl sulfide with dihydroxyfumaric acid/oxygen or ascorbic acid/oxygen as oxidants
Published in Biotechnology and bioengineering (20-02-1999)“…The chloroperoxidase catalyzed oxidation of methyl phenyl sulfide to (R)‐methyl phenyl sulfoxide was investigated, both in batch and membrane reactors, using…”
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14
Enantioselective synthesis of tert-butyl tert-butanethiosulfinate catalyzed by cyclohexanone monooxygenase
Published in Chirality (New York, N.Y.) (2001)“…Cyclohexanone monooxygenase from Acinetobacter calcoaceticus catalyzes the asymmetric oxidation of tert‐butyl disulfide to enantiomerically pure (R)‐tert‐butyl…”
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15
Microbiological transformations 35: Enantioselective one-step preparative scale synthesis of 1,3-dithiane-1-oxide via whole-cell bacterial oxidation
Published in Tetrahedron letters (19-08-1996)“…This work describes the preparative scale enantioselective oxidation of 1,3-dithiane to the corresponding monosulfoxide using whole-cell cultures of two…”
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16
Enantio and diastereoselectivity of cyclohexanone monooxygenase catalyzed oxidation of 1,3-dithioacetals
Published in Tetrahedron: asymmetry (01-02-1996)“…The asymmetric oxidation of 2-substituted dithianes, dithiolanes and oxathiolanes catalyzed by cyclohexanone monooxygenase (CMO) has been examined. The…”
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17
Enantioselective synthesis oftert-butyltert-butanethiosulfinate catalyzed by cyclohexanone monooxygenase
Published in Chirality (New York, N.Y.) (2001)Get full text
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18
Sulphoxidation reaction catalysed by myeloperoxidase from human leucocytes
Published in Biochemical journal (01-10-1998)“…The oxidation of alkyl aryl sulphides by myeloperoxidase (MPO) at the expense of hydrogen peroxide was investigated under steady-state conditions. The sulphide…”
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Enantioselective oxidations catalyzed by diketocamphane monooxygenase from Pseudomonas Putida with macromolecular NAD in a membrane reactor
Published in Biotechnology letters (01-10-1996)“…Several sulfides and bicyclo[3.2.0]hept-2-en-6-one were enantioselectively oxidized to the corresponding sulfoxides and oxa lactones by a crude preparation of…”
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20
Effects of chloride on the kinetics and stereochemistry of chloroperoxidase catalyzed oxidation of sulfides
Published in Biochimica et biophysica acta (14-12-1994)“…At pH 3, chloride dramatically influenced both the Km of chloroperoxidase (CPO) for methyl p-tolyl sulfide, which decreased, and its activity, which increased…”
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